CA2423851C - Aluminum-zirconium antiperspirant salts with high peak 5 a1 content - Google Patents

Aluminum-zirconium antiperspirant salts with high peak 5 a1 content Download PDF

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CA2423851C
CA2423851C CA002423851A CA2423851A CA2423851C CA 2423851 C CA2423851 C CA 2423851C CA 002423851 A CA002423851 A CA 002423851A CA 2423851 A CA2423851 A CA 2423851A CA 2423851 C CA2423851 C CA 2423851C
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aluminum
antiperspirant salt
peak
salt
antiperspirant
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CA2423851A1 (en
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Angel L. Carrillo
Richard Oryszczak
Yan-Fei Shen
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Gillette Co LLC
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Gillette Co LLC
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q15/00—Anti-perspirants or body deodorants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/28—Zirconium; Compounds thereof
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G25/00—Compounds of zirconium
    • C01G25/006—Compounds containing, besides zirconium, two or more other elements, with the exception of oxygen or hydrogen
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2002/00—Crystal-structural characteristics
    • C01P2002/80—Crystal-structural characteristics defined by measured data other than those specified in group C01P2002/70
    • C01P2002/87—Crystal-structural characteristics defined by measured data other than those specified in group C01P2002/70 by chromatography data, e.g. HPLC, gas chromatography
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S424/00—Drug, bio-affecting and body treating compositions
    • Y10S424/05—Stick

Abstract

Disclosed are enhanced efficacy aluminum-zirconium antiperspirant salt compositions which exhibit an HPLC peak 5 area content of about 33 % or more, preferably at least 45 %, more preferably at least 50 %, most preferably at least 55 %.
Especially preferred are aluminum-zirconium antiperspirant salt compositions which, in addition to the aforementioned high peak 5 content, also exhibit an HPLC peak 4 to peak 3 area ratio of at least 0.4, preferably at least 0.7. The aforementioned salt compositions will preferably have a metal (Al + Zr) to chloride (or anion) ratio of about 0.90 to about 1.00. Also disclosed are methods of making such antiperspirant salt compositions and aqueous solutions of such antiperspirant salt compositions. Further disclosed are topical compositions comprising a dermatologically acceptable carrier vehicle and a perspiration reducing effective amount of an aluminum-zirconium antiperspirant salt composition as described above.

Description

Aluminum-Zirconium Antiperspirant Salts With High Peak 5 Al Content The present invention relates to aluminum-zirconium antiperspirant salts with high peak 5 aluminum content. The present invention also embraces methods of making these antiperspirant salts and compositions containing these antiperspirant salts.

Aluminum-zirconium:.antiperspirant salts have been known for several decades. See, for example, US 2,814,585 (Daley), US 2,854,382 (Grad), GB 1,353',916.(Bolich), US 4,331,609 (Orr), USA;775;528 (Callaghan), US 4,871,525:(Giovanniello), US 4,900,534'(Inward), US 5,225,187 (Carmody), US 5,296,623 (Katsoulis), .US.5,330,751 (Curtin), EP 653,203 (Rosenberg), US 5,718,876 (Parekh) and US 5,955,064 (Giovanniello). Some of these aluminum-zirconium..antiperspirant. salts-aredescribed as having,enhanced efficacy, which means that they provide greater sweat reduction than conventional antiperspirant salts.

.1.5, The enhanced:efficacy salts are typically differentiated from conventional antiperspirant salts byxefe.rence to the various aluminum peaks that can be identified when the salt is analyzed by size exclusion chromatography, typically HPLC (high pressure liquid chromatography). A suitable chromatographic technique must be capable of resolving the Al into at least four distinct peaks (labeled peaks 2 (or 1+2), 3, 4 and 5, ), such as is shown in US 5,330,751. Up to now, the enhanced efficacy salts have been described as having an increased peak 4 content or an increased peak 4 to peak 3 ratio compared to conventional salts. (In some cases, enhanced salts have been described as having increased "band III" content by some~authors, depending on the chromatographic technique and nomenclature employed. Generally, bands I, II, III and IV 'of-one system correspond to peaks 1+2 (band I), 3, 4'and 5 ofthe other system.) Typically, the known enhanced efficacy salts (measured as 10% solutions) have an HPLC peak 4 to peak 3 area ratio of 0.5 or higher, preferably at least 0.7, with at least 70%, preferably at least 80%, of the aluminum contained in peaks 3 and 4. Thus, the enhanced salts will typically have a peak 4 content of at least 30% of the total aluminum contained in all the peaks (measured by peak area). In contrast, conventional non-enhanced antiperspirant salts have a negligible peak 4 content or a peak 4 to 3 area ratio less than 0.2, typically about 0.1.

Up to now, no one has suggested that peak 5 content plays any role in promoting the efficacy of antiperspirant salts. Aluminusn.antiperspirant.salts are available as 2/3, 3/4, and 5/6 aluminum chlorohydrate ("ACH") depending on the-Al.:C- ratio, (Al:CI.--4; 1.7 and:2, respectively):- Whiie<2/3 ACH - has:
a. higher..
peak 5 content (typically greater than 50%) thari 5/6 ACH (typically under 10%), .= it is not knoovn to:have greater antiperspirant efficacy... (See, for example, Bretschneider et al, "Antiperspirarit Effieacy",. in Proceedings of the 9th IFSCC
Congress, Boston, MA,1976, pp. 263-75.) In fact, 5/6 ACH is the form used virtually exclusively in commercial antiperspirant products which contain ACH.

Of course, the most widely used antiperspirant products contain aluminum-zirconium salts because they are more efficacious; especially the enhanced forms, as described above, with high peak 4 to peak 3 ratio. Prior to the discovery of the enhanced Al-Zr salts, US 4,331,609 suggested that Al-Zr salts with a metal to chloride ratio below about 1.3 (e.g., 1.25) may be more efficacious than salts with a higher metal to chloride ratio. However, this efficacy claim does not appear to have gained acceptance in the industry because salts with low metal to chloride ratios are not believed to have been produced in commercial quantities, at least not to any significant extent.
More recently, US 6,126,928 described certain polyhydric alcohol solutions of the salts described in the aforementioned '609 patent.
-2-
3 PCT/US01/46112 Generally, all of the commercially used aluminum-zirconium antiperspirant salts have a peak 5 content of less than 25%, more typically less than 10%. Recently, Westwood Chemical has introduced an aqueous aluminum-zirconium chlorohydrate solution (sold under the tradename WZR
35BX3), which is said to have stable viscosity (i.e. viscosity does not increase significantly during normal storage) and appears to be made in accordance with US 5,955,064. This salt has a somewhat elevated peak 5 content in the 20-25%
range and a relatively low peak 4 content, typically less than 15%.

The enhanced efficacy aluminum-zirconium antiperspirant salts which .10 are currently available commercially have one significant drawback. They are unstable in..aqueous. solution,..where they rapidly revert back to their non-enhanced state (for example, as evidenced by a significant drop in the HPLC
peak 4 to peak 3 area ratio). .Consequently;.these ,enhanced antiperspirant salts are generally only available in powder form and must be formulated into finished formulations as suspended powders in order to retain their enhanced .effkacy: Orie solution- to this problem is disclosed in US 6,042,816, where=stable aqueous solutions are prepared containing a calcium salt in addition to the antiperspirant salt and an amino acid..

It would be highly desix:able:to,provide enhanced efficacy aluminum-zirconium antiperspirant salts which are stable in aqueous solution. This would make it possible to use the enhanced salts in finished formulations that require an aqueous salt form, such as the currently attractive clear gel compositions which have been successfully introduced in recent years. It would also be highly desirable to provide an aluminum-zirconium antiperspirant salt which has even greater antiperspirant efficacy than those currently available.
The present inventiorLembraces enhanced efficacy aluminum-zirconium yi.
antiperspirant salt compdsitions which exhibit an HPLC peak 5-area content of about 33% or more, preferably at least 45%, more preferably at least 50%, most preferably at least 55%. Especially preferred are aluminum-zirconium antiperspirant salt compositions which, in addition to the aforementioned high peak 5 content, also exhibit an HPLC peak 4 to peak 3 area ratio of at least 0.4, preferably at least 0.7, most preferably at least 0.9. The aforementioned salt compositions will preferably have a metal (Al + Zr) to chloride (or anion) ratio of about 0.90 to about 1.00, more preferably about 0.90 to about 0.98, most preferably about 0.90 to about 0.96. The present invention also embraces methods of making such antiperspirant salt compositions and aqueous solutions of such antiperspirant salt compositions. The present invention further embraces topical compositions comprising a dermatologically acceptable carrier and a perspiration reducing. effective amount of an. aluminum-zirconium antiperspirant salt composition as. descr.ibed. above..

It has been surprisingly found that aluminum-zirconium antiperspirant s.alts with high peak 5 content (i.e. greater than 33%, preferably greater than 45%) are. at least, e-quivalent in antiperspirant efficacy to =currently available enhanced efficacy salts (with high peak 4 content) in powder form. However, unlike the currently available:.enhanced salts which lose efficacy in aqueous .solution, the high peak 5 salts maintain their enhanced efficacy as aqueous solutions. Moreover; if the high peak 5 salts also have a peak 4 to 3 area ratio of at least 0.4, they have even greater antiperspirant efficacy than currently available enhanced salts. This is very surprising because, although such salts have a high peak 4 to 3 ratio, they have a much lower total peak 4 content than conventional enhanced salts because most of the aluminum is,_present in peak 5.
Conventional enhanced Al-Zr salts typically have at least 70%, more typically about 80% to 90%, of the aluminum in peaks 3 and 4. The salts of the present invention, with high peak 5 content, have less than 67%, typically about 20%
to about 50%, of the alumirimn- in peaks 3 and 4.
-4-Fig. 1 is an HPLC chromatogram of a conventional enhanced efficacy aluminum-zirconium tetrachlorohydrate-gly antiperspirant salt (Al:Zr = 3.6;
M:C1= 1.4; peak 4:3 = 1.3; peak 5 = 17%).

Fig. 2 is an HPLC chromatogram of a high peak 5 enhanced efficacy aluminum-zirconium octachlorohydrate-gly antiperspirant salt of the present invention (Al:Zr = 6.2; M:C1= 0.95; peak 4:3 = 1.1; peak 5= 71.7%).

The present invention embraces enhanced efficacy aluminum-zirconium antiperspirant salt compositions which, when analyzed by HPLC at about 10%
(USP) concentration in.water, exhibit an HPLC peak.5 area content ofat.least 33% or.more, preferably. at1east..45%. or.mor.e,..more.prefer.ably at.least.
5.0%.or more, most preferably at least 55% or more (up to about 80%, or even as high as 90%), based on the total aluminum in the salt (as-shown in HPLC peaks 2 to 5).
The AT_"Zr salts-will. generally:have,'the empirical:formula A1nZr(OH)[3n+4_m(õ+t)](X)[m(n+.i)]-(AA)q where X is Cl, Br, I or NOs, preferably Cl;
n is 2.0 to 10.0, preferably 3.0 to 8:0; m is 0.48 to 1.11 (which corresponds to a metal (Al+Zr) to anion (X) ratio M:X=2.1-0.9), preferably about 1.00 to about 1.11 (which corresponds to M:X=1.00-0.90), more preferably about 1.02 to about 1.11 (which corresponds to M:X=0.98-0.90), and most preferably about 1.04 to about 1.11 (which corresponds to M:X=0.96-0.90); q is about 0.8 to about 4.0, preferably about 1.0 to 2.0; and AA is an amino acid such as glycine, alanine, valine, serine, leucine, or aminobutyric acid, preferably glycine. These salts also generally have some water of hydration associated with them, typically on the order of 1 to 5 moles per mole of salt (typically, about 1% to about 16%, more typically about 4% to about 13% by weight). A preferred antiperspirant salt is an aluminum-zirconium chlorohydrate (i.e. X is Cl), more preferably an aluminum-zirconium tetrachlorohydrate (Al:Zr = 2-6; M:Cl = 0.9-1.5) or aluminum-zirconium octachlorohydrate (AI:Zr = 6-10; M:Cl =- 0'.9~4.5);
especially one with a metal to chloride ratio of about 0.90 to 1.00.

In addition to having a high peak 5 content, it is also preferred, for maximum efficacy, that the Al-Zr salt have an HPLC peak 4 to peak 3 area ratio of at least 0.4, preferably at least 0.7, and most preferably at least 0.9.
Generally, a substantial portion of the balance of the aluminum not contained in peak 5 should be present in peaks 3 and 4 (that is, substantially all of the aluminum is found in peaks 3, 4 and 5). Thus, about 15% to about 67%, preferably about 20% to about 50%, of the aluminum will be present in peaks 3 and 4. In other words, the HPLC peak 3 plus peak 4 areas will comprise about 15% to about 67%, preferably about. 20%. to. about.55.%, ..moxe .preferably..
about 20% to about 50%, of HPLC peaks 2 to 5.

The A1=Zr salt compositions of the present invention are manufactured by mixing an aqueous solution of an aluminum antiperspirant salt (preferably ari enhanced aluminum,antiperspirant salt as described below) with an aqueous solution'of a zirconium antiperspirant salt, each salt being present in an amount to- provide the desired Al:Zr molar ratio, then adjusting the metal:anion (M:X) ratio, if necessary, by addition of an appropriate amount of HX. In order to drive the conversion of the aluminum polymer species toward the lowest molecular weight species which is found in peak 5, it is preferred to maintain a low metal (Al + Zr) to anion (X) ratio, typically M:X <_ 1 (e.g. 0.90 to 1.00, preferably 0.90 to 0.98), during the mixing of the aluminum and zirconium salt solutions. Typically the conversion.will take about 0.5 to 5 hours at room temperature (20-25 C): The aqueous solution of Al-Zr salt with high peak 5 content may be used or stored as an aqueous solution, or it may be spray dried or vacuum dried to obtain the salt in solid powder form. Preferably, the salt will be dried to a solid while the peak 4:3 area ratio is above 0.4 to obtain a salt with maximum efficacy. Since the peak 4:3 ratio will decrease with time in solution, while the peak 5 content increases, it is a simple matter to monitor the
-6-Al peak content- via HPLC over time and select a'point to dry the salt where both the peak 5 content and the peak 4:3 ratio are at optimum high levels.

Preferred aluminum salts for use as starting materials are those having the general formula A12(OH)s_aXa wherein X is Cl, Br, I or NO3, and a is about 0.3 to about 5, preferably about 0.8 to. about 2.5, more preferably about 1 to about 2 (such that the Al to X mole ratio is about 0.9:1 to about 2.1:1).
These salts generally have some water of hydration associated with them, typically on the order of 1 to 6.moles per mole of salt. Most preferably, the aluminum salt is aluminum-chlorohydrate (i.e. X is Cl in the above formula), especially 5/6 basic aluminum chlorohydrate where a is about 1, such that the aluminum to chlorine mole ratio is about 1.9:1 to 2.1:1, typically about 1.95:1. Aluminum chlorohydrate is referred to as "ACH" herein.
,., Preferably; the ACH is an enhanced e~cacy form, sometimes written as ACH',-which has an HPLC peak 4 to peak 3 area ratio of at least 0.5, preferably 15. at least.Ø7, with. at.least 70%, preferably at least 80%, of the aluminum contained in peaks _3 and 4. The erihanced 'efficacy aluminum chlorohydrates are readilymade.by heating a dilute ACH solution (e.g. about 10% salt concentration-by weight)~.at" about 80-100 C for about 4 to 20 hours. It has been found that the greatest antiperspirant efficacy in the final Al-Zr antiperspirant .20 salt with high peak 5 can be obtained when an enhanced efficacy aluminum antiperspirant salt is used as one of the starting materials.

Preferred zirconium salts for use as starting materials are those having the general formula Zr(OH)4-bXb wherein X is Cl, Br, I, or NO3, preferably Cl;
and b is about 0.7 to about 4.0, preferably about 2.2 to about 4.0 (i.e., Zr:X
-25 0.45-0.25), more preferably about 3.4 to about 3.8 (Zr:X = 0.29-0.26).
Although written for convenience as Zr(OH)4.._bXb, this salt is intended to include the well-known zirconyl oxychloride and zirconyl hydroxychloride, which is also often written as ZrO(OH)2_bClb (where b, in this instance, is about 1 to 2)_.The
-7-zirconium salts also generally have some water of hydration associated with them, typically on the order of 1 to 7 moles per mole of salt. In addition, the zirconium salt will contain an amino acid, as described above, to prevent gellation. Preferably the zirconium salt is zirconyl hydroxychloride of the formula Zr(OH)4_bClb wherein b is about 0.7 to about 4.0, preferably about 2.2 to about 4.0 (i.e., Zr:Cl ` 0.45-0.25), more preferably about 3.4 to about 4.0 (Zr:C1= 0:29-0.25), most preferably about 3.4 to about 3.8 (Zr:C1= 0.29-0.26).
Zirconium salts with a low Zr:X ratio are preferred because such salts tend to have a lower molecular weight than other zirconium salts. It is theorized that the use of low molecular weight zirconium salts results in higher antiperspirant efficacy in the final Al-Zr salt. In addition, the use of zirconium salts with a low Zr:X ratio also facilitates the manufacture of the preferred AI-Zr, salt with a low metal:X ratio.:

As an alternative to=or in conjunction with the above-described aluminum and zir.conium salts,.it is. also.possible. to e.mplo.y aluminum chloride (AICIs) and/or.zirconiuiri basic-carbonate (Zr2(O.H)4'(CO3)2`nH2O) as starting materials, provided that the molar'ratio of the various reactants is adjusted to arrive at the desired molar ratio of the aluminum, zirconium, hydroxyl and chloride moieties in the final Al-Zr salt prepared.

A preferred high peak 5 enhanced salt is aluminum-zirconium chlorohydrate (i.e. X is Cl), referred to herein as "E5AZCH", which has an Al:Zr ratio of about 2 to about 10 and a metal: CI ratio of 0.90 to 1.00, preferably 0.90 to 0.98. This salt will exhibit an HPLC peak 5 area content of about 45% or more, preferably at least 50% or more, more preferably at least 55% or more, up to about 90%, based on the total aluminum in the salt. To achieve maximum efficacy, this salt will also preferably have an HPLC peak 4 to peak 3 area ratio of at least 0.4, more preferably at least 0.7, and most preferably at least 0.9. It has been surprisingly found that such a salt has superior antiperspirant efficacy, and more surprisingly will maintain its superior antiperspirant
-8-efficacy, even when stored as an aqueous solution. This is a distinct advantage over previously known enhanced antiperspirant salts, whose efficacy deteriorates in aqueous solution.
The antiperspirant salts of the present invention may be formulated into topical compositions such as liquids (e.g., for roll-on or porous applicators), lotions, creams, gels, soft-solids, solid sticks, etc. Such compositions will comprise the antiperspirant salt in a perspiration reducing effective amount and a dermatologically acceptable carrier.
In particular, aqueous solutions of these antiperspirant salts may be directly utilized in oil-in-water and water-in-oil emulsions, such as the currently popular clear gel formulations, or in other aqueous based compositions such as aqueous based roll-ons.
Preferred aqueous liquid compositions will comprise about 8% to about 45 %
(USP) by weight, preferably about 18 % to about 38 % (USP) by weight, antiperspirant salt and about % to about 90 %, preferably about 45 % to about 80 %, water, such aqueous compositions optionally including other water soluble cosmetic ingredients (e.g. ethanol or polyhydric 15 alcohol). These aqueous solutions may be stored indefinitely without significant loss of efficacy, unlike solutions of conventional enhanced efficacy salts, and may be diluted to an appropriate concentration (e.g. 6%-22 % USP) for topical application when formulated into a commercial product.
It is also possible to make a solution of ESAZCH in a liquid polyhydric alcohol such 20 as propylene glycol. The liquid polyhydric alcohol will typically have from three to six carbon atoms and from two to six hydroxyl groups. Such a solution may be readily obtained by adding the polyhydric alcohol to an aqueous solution of ESAZCH as described above, then evaporating off the water under vacuum (see, for example, US 5,643,558).
Such a polyhydric alcohol composition may advantageously comprise about 8% to about 45 % (USP) of said antiperspirant salt. This product can then be readily formulated into topical antiperspirant compositions which use a polyhydric alcohol vehicle, such as
-9-clear sticks gelled with dibenzylidene sorbitol or other gellants (see, for example, 5,705,171).

It is especially preferred to produce the E5AZCH salts of the present invention in solid powder form, for example by spray drying or vacuum drying the aqueous solution in which these salts are produced. The powdered antiperspirant salts may then be formulated into any known type of topical composition which utilizes powdered salts, including, in particular, liquid roll-on, cream, soft solid and solid stick formulations in which the powdered salt is suspended in an anhydrous, dermatologically acceptable carrier, particularly, a carrier.comprising a silicone (e.g. cyclomethicone, dimethicone, etc.), typically at a.concentr.ation.of about 6% to about.22% (USP) active by weight.

The present invention also embraces a method. of inhibiting or reducing perspiration"by topically applying-an effective amount of an antiperspirant' composition as described herein to the skin of a human, preferably to the axilla, where such reduction.in' perspiration.is, desired by the. user. An effective amount is that'amount which provides'at least a 20% sweat'reduction, preferably at ieast.a 40% sweat reduction, when tested in accordance with a standard hot.,room.thermal efficacy.protocol, and most preferably that amount which reduces per.spirationto a degree that is noticeable by the user.
Typically, the amount of antiperspirant composition applied will range from about 0.1 gram to about 1.0 gram per axilla depending on the formulation or such amount as will deliver about 0.01 to about 0.25 gram of antiperspirant active per axilla.
The present invention may be further illustrated by the following examples in which the parts and percentages are by weight. In these examples, the abbreviation ACH means standard efficacy (i.e. non-enhanced) 5/6 basic aluminum chlorohydrate with. an -AI:Cl ratio of about 1.95. Unless otherwise stated, the ACH used in the examples has a concentration of about 42% USP
active (nominally 50% by weight). The abbreviation ACH'. means an enhanced efficacy form of this salt, that is one having an HPLC peak..4 ta peak 3 area
-10-ratio of at least 0.7 with at least 80% of the aluminum contained in-peaks 3 and -4. The ACH' is made by diluting ACH with water to form a solution of about 10% concentration, heating the dilute ACH solution at about 85 C for about 16 hours, then rapidly concentrating the ACH' by vacuum evaporation (for example, using a falling film evaporator) to a concentration. of about 42% USP
active and cooling to room temperature. The ACH' must be used within several hours of preparation, preferably as soon as possible after preparation, in order to insure that it has the desired high peak 4 to peak 3 ratio.

The abbreviation ZHCG means zirconyl hydroxy chloride-glycine (Zr:Gly = 1). When.referring to this material, the Zr:Cl ratio (e.g. Zr:C1=
0.28) will be indicated in,parentheses following .the, abbreviation.. The ZHCG.
may.be.
prepared by reacting zirconium basic carbonate with an appropriate.amount of HCI to -achieve the- desired= Zr:Cl.ratio; then:adding the appropriate=amouut of:, -glycine_ . The.aqueous ZHCG.used in the examples has a Zr content of about 8%
(Zr: Cl = 0.26), to .about 19%(Zk:Ct =- 1..1). by weight Zr.

The abbreviation AZCH meains. aluminum-zirconium chlorohyd.rate-gly (standard efficacy), EAZCH means.a conventional enhanced efficacy AZCH with high peak 4:3 ratio, and E5AZCH means an enhanced efficacy AZCH of the present invention with high peak 5.

Comparative Example In accordance with the technique described in US 4,775,528, freshly prepared aqueous ACH' solution is mixed with aqueous ZHCG" (Zr:C1= 0.67) in the appropriate molar ratio to provide an aqueous solution of enhanced efficacy aluminum-zirconium tetrachlorohydrate (-33%USP) with an Al:Zr mole ratio of about 3.6 and a M:Cl mole ratio of about 1.4. This solution is spray dried to obtain the EAZCH salt in solid powder form. A sample of this antiperspirant salt, when dissolved in water at about 10% concentration and analyzed by HPLC within a few minutes of preparation, produces a chromatogram as shown
-11-in Fig. 1. From this chromatogram, it can- be-seen that more than-80% of the aluminum is contained in peaks 3 and 4, with the peak 4:3 area ratio being about 1.3, while the amount of peak 5 aluminum is about 17% of the total aluminum. As is well-known, this salt cannot be usefully employed in aqueous, form because the peak 4:3 ratio deteriorates very quickly, thus reverting to a standard efficacy salt.

The above-described enhanced efficacy salt may be tested for,thermal efficacy (i.e. hot room sweat reduction) using volunteer panelists in a standard hot room protocol. The test product (vehicle plus enhanced efficacy salt) is ,10 applied to one axilla and control product (vehicle only or vehicle plus standard efficacy antiperspirant salt) is applied to the other axilla. The. above-described.
enhanced efficacy salt typically provides a sweat reduction of about 57-62%
versuR about 47-52%-obtained:with standard.,efficacy salt,:whensuspended-as= , an 18-19% USP active in a liquid volatile silicone carrier vehicle. Also, a freshly prepared aqueous solution of the above-describe-d enhanced efficacy salt (20%
USP active) -typically proVides a sweat. reduction-of about 63-69% versus about 48-54% obtained with standard efficacy salt in aqueous solution at the same concentration.

Example 1 Freshly prepared aqueous ACH' solution (or in one case, sample H, standard ACH solution) is mixed with aqueous ZHCG solution (as defined below) in the appropriate molar ratio to provide the desired Al:Zr ratio along with sufficient HCl, as needed, to provide the desired M:Cl ratio, thus forming aqueous solutions of enhanced efficacy aluminum-zirconium chlorohydrates (about 30-35% USP active) with Al:Zr mole ratios, M:CI mole ratios, and HPLC
peaks as shown in Table 1 below. The various ZHCG solutions used are as follows: ZHCGb (Zr:C1= 0.26-0.28), ZHCG' (Zr:C1= 0.44-0.45), and ZHCGd (Zr:C1= 0.44-0.45), the ZHCGd being a blend of about 60 parts ZHCGb and
-12-about 40 parts ZHCGf '(Zr:Cl = 1:05=t:10). A portion of each antiperspirant-saIt -solution is retained for further testing, and the remainder is spray dried to recover the antiperspirant salt as a powder. Antiperspirant salt B, when diluted to about 10% concentration, produces an HPLC chromatogram as shown in Fig. 2.

Table 1 Enhanced Al-Zr Salts With High Peak 5 E,5AZCH ZHCG Al:Zr M:Cl Peak 5 Peak 4:3 A b 10 0.94 53.9 0.41 B1 b 6.2 0.95 71.7 1.1 C b 10 0.94 53.7 0.46 D d 2 0.92- 51.8 1.9 E c 2.1 0.95 48.5 2.4 F d 2 0.92 57.7 1.72 G2 d 2 0.9 74.7 0.17 H3 d4 2 0.94 57.2 0.2 J b 4.6 0.96 50.0 1.7 K b 7.8 1.15 33.7 2.0 1 Aged 1.5 years as aqueous solution (-33% USP) 2 Heated at 70 C for 24 ho.urs after mixing components to reduce the peak 4:3 ratio 3 Made with standard ACH (peak 4:3 ratio <0.2) 4 Zr:C1= 0.47 by blending ZHCGb (Zr:C1= 0.28) and ZHCGa (Zr:C1= 0.67) Example 2 The above-described high peak 5 enhanced efficacy salts of Example 1 are tested for thermal efficacy (i.e. hot room sweat reduction) using volunteer panelists in a standard hat room protocol. The test product is applied to one axilla and control product is applied to the other axilla in an AvB
comparison.
In all cases, the test product comprises vehicle (as described below),plus high peak 5 enhanced efficacy salt (E5AZCH). The control product comprises.
vehicle'
-13-plus conventional enhanced efficacy (higii peak 4:3) antiperspirant salt (EAZCH), except where the vehicle is a clear gel formulation, in which case a standard efficacy salt (AZCH) is used because of the instability of the conventional enhanced salt in aqueous formulations. To counteract this instability, the formulation identified as "Aqueous" below, is freshly prepared with powdered EAZCH just prior to being tested. The formulations tested are set out below and the results are shown in Table 2. The results are reported as the average sweat reduction ("S.R.") gain over the control (i.e. the absolute percentage point increase in sweat reduction over the control).

Aqueous Roll-On 20% USP AP active 20.0% AP active q.s. water 75,1% Cyclomethicone 3.5% Quaterni.um-18 hectorite 1.0% Propylene carbonate .4% Fragrance Clear Gel Solid 23.5% AP active 23.5% AP active 39.8% Water 51.9% Cyclomethicone 8.7% Propylene Glycol 13.5% Stearyl alcohol - 10.0% Ethanol - 3.0% Hydrogenated castor oil 9.7% Dimethicone 4.0% Myristyl myristate 8.1% Cyclomethicone (and) 1.8% Silica Dimethicone copolyol 2.3% Fragrance/ Silk Powder 0.2% Fragrance
- 14-Table 2 Thermal Efficacy of Al-Zr Salts With High Peak 5 E5AZCH Vehicle Control Avg. S.R. Gain Over Control A Roll-On EAZCH 5.8 (p=0.0001) B Aqueousl EAZCH 7.0 (p=0.004) C Aqueous EAZCH 4.2 (p=0.025) C Clear Gel AZCH 15.9 (p=0.0001) C Clear Gel2 AZCH 13.3 (p=0.0001) D Aqueous EAZCH 5.9 (p=0.0001) D Aqueous EAZCH 4.6 (p=0.002) D Roll-On EAZCH 8.7 (p=0.0001) E Aqueous EAZCH 1.3. (N.S.)4.
F Aqueous EAZCH 4.5 (p=0.059) F Solid .. . EAZ.CH. 4.Ø -(p-0_012).
G3 Solid EAZCH 2.1 (N.S.) H3 Aqueous EAZCH 0.3 (N.S.) J Aqueous EAZCH 4.3 (p=0.001) K Aqueous EAZCH ' 1.7 (N.S.) i Aged 1.5 years 2 Aged 3 months at 45 C. (HPLC of extracted salt: peak 4:3 = 0.47; peak 5 65.8) 3 Low peak 4:3 ratio (0.2) 4 N.S. = not significant From the above data, it can be seen that the preferred enhanced antiperspirant salts of the present invention (high peak 5 and peak 4:3 >0.4;
e.g. salts A, B, C, D, F and J) are more efficacious than conventional enhanced antiperspirant salts (high peak 4:3 ratio, but low peak 5). This result is surprising because the amount of aluminum contained in peaks 3 and 4 of the E5AZCH salt is considerably reduced versus the EAZCH (<50% vs. >80%). Even more surprising is the fact that the E5AZCH salt (salt B) retains its superior efficacy when stored as a concentrated aqueous solution (in this case, for 1.5
-15-years). Conventional enhanced salts lose their enhanced state in aqueous solution.
When formulated as a clear gel, the high peak 5 salt (salt C) is substantially more efficacious than the current commercial clear gel product, which must use a standard efficacy salt, and this high peak 5 salt maintains its high efficacy even after storage of the clear gel at high temperature. In addition, the high peak 5 salts with low peak 4:3 ratio (salts G and H) are surprisingly just as efficacious as the conventional enhanced salt with high peak 4:3 ratio. Such salts, while not quite as efficacious as the preferred salts, can provide a useful alternative to the currently available enhanced salts, particularly where improved efficacy is desired in aqueous based formulations where current enhanced salts cannot be used. Similarly, salt K, with only a modest peak 5 content (peak 5 =
33 .7 %) is just as efficacious as a conventional enhanced salt and could be an advantageous alternative, particularly in aqueous based formulations. Although salt E
proved to be just as efficacious as the conventional enhanced salt and would thus offer the same advantage as salts G and H, it is believed that further testing would reveal that an ESAZCH
with a peak 5 content of 48 % would be somewhat more efficacious than a conventional enhanced salt.
Throughout the specification reference to HPLC analysis means that chromatograms are obtained as follows: Salt solutions are evaluated for aluminum polymer distribution by HPLC at a concentration of about 10% (USP) Al-Zr salt. If the solution to be analyzed is at a higher salt concentration, it is diluted with sufficient water to bring the salt concentration to about 10%. A 1.O L sample is injected into a Waters U6KT""
injector, then pumped through a 4.6mm X 500mm column packed with NucleosilTM 100-5 silica with pore size of 100 angstroms and particle size of 5,2m (Keystone Scientific Inc.) using a 0.01M aqueous nitric acid solution as the eluant. The flow rate of the mobile phase is controlled at 0.5mL/min with an LDC/Milton Roy Constametric-IIT^^ metering
-16-pump (ThermoQuest Inc.). HPLC profiles are recorded and processed with a computerized system that includes the Millennium 32TM Chromatography Manager software from Waters Corp. A Waters 2410TM differential refractometer is used as the refractive index detector. The HPLC profiles are read from left to right (higher to lower molecular weight). Following this technique, peak 3 typically appears at a retention time of about 11.0-12.0 minutes (Kd = 0.58-0.61), peak 4 typically appears at a retention time of about 11.9-12.9 minutes (Kd = 0.62-0.72), and peak 5 typically appears at a retention time of about 13.3-14.0 minutes (Kd a5 0.83-0.91). Naturally, of course, other HPLC
techniques which use different column materials, eluants and flow rates can be used provided that they sufficiently resolve peaks 3, 4 and 5 with an acceptable degree of precision (i.e. the technique must be capable of resolving the Al into at least four distinct peaks, with the first Al peak being labeled peak 2 or peak 1+2). Obviously, such other techniques may place peaks 3, 4 and 5 at different retention times from those given above.

It should be noted that reference throughout this application to weight percent of antiperspirant salt is intended to be calculated as anhydrous weight percent in accordance with the new U.S.P method. This calculation excludes any bound water and glycine. For aluminum-zirconium chlorohydrate, the calculation is as follows:

%AZCH = %Al{26.98y + 92.97 + 17.01[3y+4-(y+1)/z] + 35.45(y+l)/z} / 26.98y where y = Al/Zr ratio and z = metal/Cl ratio.

For reference purposes, calculation of antiperspirant salt weight percent in accordance with the U.S.P. method compares to the previously used standard industry method as follows:
50% AZCH (std) ~- 38.5% USP.
-17-

Claims (37)

CLAIMS:
1. An aluminum-zirconium antiperspirant salt having the formula Al n Zr(OH)[3n+4-m(n+1](X)[m(n+1))-(AA)q wherein:

X is Cl, Br, I or NO3, n is 2.0 to 10.0, m is 0.48 to 1. 11, q is 0.8 to 4.0, and AA is an amino acid;

wherein the aluminum-zirconium antiperspirant salt is prepared using a zirconium salt of the general formula Zr(OH)0-1.8X2.24; and wherein said salt, when analyzed by HPLC as a 10 wt % aqueous solution using conditions capable of resolving the aluminum into at least four successive peaks exhibits an HPLC
peak 5 as shown in Figure 2 which has an area of at least 33 % or more based on the total area of HPLC peaks 2 to 5.
2. The antiperspirant salt of claim 1 wherein said HPLC peak 5 area is at least 45%.
3. The antiperspirant salt of claim 1 wherein said HPLC peak 5 area is at least 50%.
4. The antiperspirant salt of claim 1 wherein said HPLC peak 5 area is at least 55%.
5. The antiperspirant salt of claim 1, 2, 3 or 4 having an HPLC peak 4 to peak 3 area ratio of at least 0.4, and wherein all of the aluminum is found in peaks 3, 4 and 5.
6. The antiperspirant salt of claim 5 wherein said antiperspirant salt is an aluminum-zirconium chlorohydrate.
7. The antiperspirant salt of claim 1 wherein the HPLC peak 5 area comprises 45% to less than 80 % and the HPLC peak 3 plus peak 4 areas comprise 20% to less than 55% of HPLC peaks 2 to 5.
8. The antiperspirant salt of claim 7 having an HPLC peak 4 to peak 3 area ratio of at least 0.4.
9. The antiperspirant salt of claim 8 wherein said antiperspirant salt is an aluminum-zirconium chlorohydrate.
10. The antiperspirant salt of claim 1 wherein said antiperspirant salt is an aluminum-zirconium chlorohydrate having a metal (Al+Zr) to chloride molar ratio of 0.90 to 1.00.
11. The antiperspirant salt of claim 10 having an HPLC peak 4 to peak 3 area ratio of at least 0.4, and wherein the aluminum is found in peaks 3, 4 and 5.
12. The antiperspirant salt of claim 11 wherein said HPLC peak 5 area is at least 45%.
13. The antiperspirant salt of claim 1 having the formula Al n Zr(OH)[3n+4-m(n+1)](Cl)[m(n+1)]-(Gly)q.
14. The antiperspirant salt of claim 13 wherein m is 1.02 to 1.11.
15. The antiperspirant salt of claim 13 wherein m is 1.04 to 1.11.
16. The antiperspirant salt of claim 13 wherein q is 1.0 to 2Ø
17. The antiperspirant salt of claim 13 having an HPLC peak 4 to peak 3 area ratio of at least 0.4.
18. An aqueous composition comprising water and, dissolved therein, an aluminum-zirconium antiperspirant salt according to any one of claims 1 to 17.
19. The aqueous composition of claim 18 comprising 8% to 45% by weight of said antiperspirant salt.
20. A composition comprising a liquid polyhydric alcohol and, dissolved therein, an aluminum-zirconium antiperspirant salt according to any one of claims 1 to 17.
21. The composition of claim 20 comprising 8% to 45% by weight of said antiperspirant salt.
22. A clear antiperspirant gel composition comprising a water-in-oil emulsion having a water phase and an oil phase, wherein the water phase comprises an aqueous composition according to claim 18.
23. A topical antiperspirant composition comprising a dermatologically acceptable carrier and a perspiration reducing effective amount of an aluminum-zirconium antiperspirant salt according to any one of claims 1 to 17.
24. The topical antiperspirant composition of claim 23 wherein said carrier is an anhydrous carrier and said antiperspirant salt is in solid powder form suspended in said anhydrous carrier.
25. The topical antiperspirant composition of claim 24 wherein said anhydrous carrier comprises a silicone.
26. The topical antiperspirant composition of claim 23 in the form of a liquid, lotion, cream, gel, soft-solid, or solid stick.
27. A method of reducing perspiration from human skin comprising applying to human skin a topical antiperspirant composition according to claim 23.
28. A method of reducing perspiration from human skin comprising applying to human skin an aluminum-zirconium antiperspirant salt according to any one of claims 1 to 17.
29. A method of preparing an aluminum-zirconium antiperspirant salt of the formula Al n Zr(OH)[3n+4-m(n+1)](X)[m(n+1)]-(AA)q wherein:
X is Cl, Br, I or NO3, n is 2.0 to 10.0, m is 1.00 to 1.11, q is 0.8 to 4.0, and AA is an amino acid;

wherein the mole ratio of Zr to X is from 0.25 to 0.45; and wherein said salt, when analyzed by HPLC as a 10 wt % aqueous solution using conditions capable of resolving the aluminum into at least four successive peaks exhibits an HPLC
peak 5 as shown in Figure 2 which has an area of at least 33% or more based on the total area of HPLC peaks 2 to 5;

said method comprises mixing an aqueous solution of an aluminum antiperspirant salt of the formula:

Al2(OH)6-a X a wherein:

X is Cl, Br, I or NO3, and a is 1 to 2, with an aqueous solution comprising an amino acid and a zirconium antiperspirant salt of the formula:

Zr(OH)4-b X b wherein:

X is Cl, Br, I, or NO3, and b is 2.2 to 4.0, each of said aluminum antiperspirant salt and said zirconium antiperspirant salt being present in an amount to provide an Al:Zr molar ratio of 2.0 to 10.0, adjusting the metal (Al+Zr) to anion (X) molar ratio to 0.90 to 1.00 by addition of an appropriate amount of aqueous HX, and maintaining the mixture until the aluminum-zirconium antiperspirant salt formed has an HPLC peak 5 area of at least 33%.
30. The method of claim 29 comprising adjusting the metal (Al+Zr) to anion (X) molar ratio to 0.90 to 0.98.
31. The method of claim 29 wherein X is Cl for both the aluminum and zirconium salts and b is 2.2 to 4Ø
32. The method of claim 31 wherein b is 3.4 to 4Ø
33. The method of claim 31 comprising adjusting the metal (Al+Zr) to anion (X) molar ratio to 0.90 to 0.98.
34. The method of claim 32 comprising adjusting the metal (Al+Zr) to anion molar ratio to 0.90 to 0.98.
35. The method of any one of claims 29 to 34 wherein said aluminum antiperspirant salt has an HPLC peak 4 to peak 3 area ratio of at least 0.5 with at least 70% of the aluminum contained in peaks 3 and 4.
36. The method of claim 29 or 33 which additionally comprises drying said solution to obtain said aluminum-zirconium antiperspirant salt in solid form.
37. The method of claim 36 wherein said aluminum antiperspirant salt has an HPLC
peak 4 to peak 3 area ratio of at least 0.5 with at least 70% of the aluminum contained in peaks 3 and 4, and said aluminum-zirconium antiperspirant salt in solid form has an HPLC
peak 4 to peak 3 area ratio of at least 0.4 with at least 20% of the aluminum contained in peaks 3 and 4.
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Families Citing this family (86)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6436381B1 (en) 2000-10-25 2002-08-20 The Gillette Company Aluminum-zirconium antiperspirant salts with high peak 5 al content
US6726901B2 (en) 2002-05-09 2004-04-27 The Gillette Company Stabilized antiperspirant compositions containing aluminum-zirconium salts with low M:Cl ratio
US6663854B1 (en) 2002-06-19 2003-12-16 Yan-Fei Shen Aluminum-zirconium antiperspirant salts made with zirconium salts having low Zr:Cl ratio
US6960338B2 (en) 2002-06-28 2005-11-01 Reheis, Inc. Amino acid free stable aluminum/zirconium antiperspirant solution
US20040091436A1 (en) * 2002-11-12 2004-05-13 Zijun Li Antiperspirant compositions of enhanced efficacy containing strontium
US6936242B2 (en) 2002-11-15 2005-08-30 The Gillette Company Multi-portion antiperspirant composition
US20040109833A1 (en) 2002-12-09 2004-06-10 Xiaozhong Tang High efficacy, low irritation aluminum salts and related products
US6923952B2 (en) * 2003-08-14 2005-08-02 The Gillette Company Enhanced efficacy antiperspirant compositions containing strontium or calcium
US20050095210A1 (en) * 2003-10-29 2005-05-05 Jairajh Mattai Underarm products with superabsorbent component
US7060258B2 (en) * 2004-02-17 2006-06-13 Reheis, Inc. Method of making aluminum-zirconium antiperspirant of enhanced efficacy
US6902724B1 (en) 2004-03-24 2005-06-07 Reheis, Inc. Enhanced efficacy basic aluminum halides, antiperspirant active compositions and methods for making
US7014843B2 (en) * 2004-03-24 2006-03-21 Reheis, Inc. Enhanced efficacy basic aluminum halides/metal cation salt, antiperspirants actives and compositions containing such materials and methods for making
US7731943B2 (en) * 2004-07-07 2010-06-08 Summit Research Labs, Inc. Stabilized aqueous aluminum zirconium solutions
US7087220B2 (en) * 2004-05-28 2006-08-08 Reheis, Inc. High pH antiperspirant compositions of enhanced efficacy
US7153495B2 (en) * 2004-06-10 2006-12-26 Reheis, Inc. Fragrance friendly and cost effective antiperspirant actives and method of making the same
US7704531B2 (en) 2005-02-18 2010-04-27 Colgate-Palmolive Company Enhanced efficacy aluminum or aluminum-zirconium antiperspirant salt compositions containing calcium salt(s) and betaine
CL2006003116A1 (en) * 2005-11-16 2008-02-29 Colgate Palmolive Co ANTI-TRANSPIRING COMPOSITION THAT INCLUDES AT LEAST ONE CHOSEN ALUMINUM SALT, ZIRCONY ALUMINUM, A COMPLEX ALUMINUM SALT OR A COMPLEX ALUMINUM-ZIRCONY SALT, A HYDROXIACIDE AND AN ACID COMPOUND OF QUATERNARY AMMONIUM; PROCESS TO PREPARE
US8801909B2 (en) * 2006-01-06 2014-08-12 Nextchem, Llc Polymetal hydroxychloride processes and compositions: enhanced efficacy antiperspirant salt compositions
US7846318B2 (en) * 2006-01-06 2010-12-07 Nextchem, Llc Polyaluminum chloride and aluminum chlorohydrate, processes and compositions: high-basicity and ultra high-basicity products
EP2167018A2 (en) 2007-06-20 2010-03-31 Henkel AG & Co. KGaA Cosmetic stick based on a congealed oil-in-water dispersion/emulsion
DE102008028822A1 (en) 2007-06-20 2009-02-19 Henkel Ag & Co. Kgaa Cosmetic stick composition for application to the skin for treating acne, pimples, blackhead and cellulitis, and for skin tightening, comprises wax component, polymeric organic hydrogel forming substance and nonionic oil in water emulgent
WO2009039030A1 (en) 2007-09-21 2009-03-26 Colgate-Palmolive Company Oxo-hexameric zirconium-octaamino acid antiperspirant salts
US8257689B2 (en) * 2007-12-12 2012-09-04 Colgate-Palmolive Company Antiperspirant active compositions having SEC chromatogram exhibiting high SEC peak 4 intensity
US20100202993A1 (en) * 2007-12-12 2010-08-12 Long Pan Antiperspirant Active Compositions Having SEC Chromatogram Exhibiting High SEC Peak 4 Intensity
DE102007063352A1 (en) * 2007-12-28 2009-07-02 Henkel Ag & Co. Kgaa Anhydrous antiperspirant compositions with improved drug release
US20090257970A1 (en) * 2008-03-14 2009-10-15 Ernest Bloom Antiperspirant compositions containing a copper salt and a penetration enhancer and methods of using the same
DE102008035013A1 (en) 2008-07-25 2010-01-28 Henkel Ag & Co. Kgaa Anhydrous deodorant compositions with improved performance, which are administered as nonaerosol
DE102008035014A1 (en) 2008-07-25 2010-01-28 Henkel Ag & Co. Kgaa Anhydrous deodorant compositions with improved performance, which are applied as a spray
DE102008064198A1 (en) 2008-12-22 2010-07-01 Henkel Ag & Co. Kgaa Transparent antiperspirant gels
DE102009027052A1 (en) 2009-06-19 2010-12-23 Henkel Ag & Co. Kgaa Antiperspirant compositions with silver citrate
DE102009027604A1 (en) 2009-07-10 2011-01-20 Henkel Ag & Co. Kgaa Cosmetic compositions with suspensions of silver salts
WO2011016807A1 (en) * 2009-08-06 2011-02-10 Colgate-Palmolive Company Method of making an antiperspirant active composition having sec chromatogram exhibiting high sec peak 4 intensity
DE102009029423A1 (en) 2009-09-14 2011-03-24 Henkel Ag & Co. Kgaa Antibacterial cosmetic or pharmaceutical body odor deodorant compositions against body odor
US9523454B2 (en) * 2009-10-21 2016-12-20 Brasscraft Manufacturing Company Anti-rotation gripper ring
US9494268B2 (en) * 2009-10-21 2016-11-15 Brasscraft Manufacturing Company Supply stop with connection verification
DE102009055255A1 (en) 2009-12-23 2011-06-30 Henkel AG & Co. KGaA, 40589 Anhydrous antiperspirant sprays with improved performance
US9144695B2 (en) 2010-06-01 2015-09-29 Coty Inc. Antiperspirant compositions
DE102010038357A1 (en) 2010-07-23 2012-01-26 Henkel Ag & Co. Kgaa Double salt antiperspirant sticks
DE102010038356A1 (en) 2010-07-23 2012-01-26 Henkel Ag & Co. Kgaa Double salt alcoholic antiperspirants
DE102010038358A1 (en) 2010-07-23 2012-01-26 Henkel Ag & Co. Kgaa Double salt antiperspirant roll-ons
BR112013010694A2 (en) 2010-11-02 2016-07-05 Colgate Palmolive Co active antiperspirant compositions and their production
US9463985B2 (en) 2010-11-02 2016-10-11 Colgate-Palmolive Company Aluminum salt containing high percentage of Al30
DE102010063250A1 (en) 2010-12-16 2012-06-21 Henkel Ag & Co. Kgaa Hydrous antiperspirant compositions with improved residue masking
DE102011002863A1 (en) 2011-01-19 2012-07-19 Henkel Ag & Co. Kgaa Antiperspirant sticks with improved long-term stability
US9174851B2 (en) 2011-04-26 2015-11-03 Colgate-Palmolive Company Compositions containing polyhydroxyoxoaluminum cations and manufacture thereof
BR112013027593A2 (en) 2011-04-26 2017-06-20 Colgate Palmolive Co antiperspirant active compositions and their manufacture
DE102011083293A1 (en) 2011-09-23 2013-03-28 Henkel Ag & Co. Kgaa Anhydrous formulations with cooling effect
DE102011083872A1 (en) 2011-09-30 2012-06-21 Henkel Ag & Co. Kgaa Sweat-absorbing complex, useful for reducing and/or regulating perspiration and/or body odor, comprises sheet silicate which is modified with quaternary ammonium compound, and oily extract of sprouts of Bambusa vulgaris and lignocellulose
DE102011086923A1 (en) 2011-11-23 2013-05-23 Henkel Ag & Co. Kgaa Deodorising compositions
DE102011087980A1 (en) 2011-12-08 2012-09-06 Henkel Kgaa Cosmetic and non-therapeutic use of platycodin e.g. for influencing natural pigmentation process of hair and its follicles in armpit region, for reducing shaving or epilation frequency, and as active substance in topically applied agents
DE102011088967A1 (en) 2011-12-19 2013-06-20 Henkel Ag & Co. Kgaa Deodorants and antiperspirants with stabilized antioxidant
DE102011089012A1 (en) 2011-12-19 2013-06-20 Henkel Ag & Co. Kgaa Textile-friendly antiperspirants
DE102012205218A1 (en) 2012-03-30 2013-10-02 Henkel Ag & Co. Kgaa Antiperspirant compositions with cycloaliphatic diols and zirconium salts
DE102012209621A1 (en) 2012-06-08 2013-12-24 Henkel Ag & Co. Kgaa Thickened antiperspirant rollons with improved residue behavior
DE102012223197A1 (en) 2012-12-14 2014-06-18 Henkel Ag & Co. Kgaa Anhydrous compositions against body odor
DE102012224156A1 (en) 2012-12-21 2014-06-26 Henkel Ag & Co. Kgaa Textile-friendly nonaerosol antiperspirants with hydroxycarboxylic acids
DE102012224133A1 (en) 2012-12-21 2014-06-26 Henkel Ag & Co. Kgaa Textile-friendly nonaerosol antiperspirants with methanesulfonic acid
CN105246335A (en) * 2013-03-08 2016-01-13 里博科公司 Methods for treating flowering plants with ribose
DE102013211312A1 (en) 2013-06-17 2014-12-18 Henkel Ag & Co. Kgaa Anhydrous compositions
DE102013211313A1 (en) 2013-06-17 2014-12-18 Henkel Ag & Co. Kgaa Anhydrous compositions against body odor
DE102013220783A1 (en) 2013-10-15 2015-04-16 Henkel Ag & Co. Kgaa Antiperspirant cosmetic products containing alkyl sulfonic acids
DE102013220777A1 (en) 2013-10-15 2015-04-16 Henkel Ag & Co. Kgaa Antiperspirant cosmetic products with alpha hydroxy acids
DE102013220782A1 (en) 2013-10-15 2014-04-17 Henkel Ag & Co. Kgaa Antiperspirant cosmetic agent comprises cosmetic oils which are liquid at specific temperature and pressure, perfumes or waxes, antiperspirant aluminum salt, and substituted benzoate salt
DE102013220779A1 (en) 2013-10-15 2015-04-16 Henkel Ag & Co. Kgaa Antiperspirant cosmetic products containing lactates
DE102013220789A1 (en) 2013-10-15 2015-04-16 Henkel Ag & Co. Kgaa Antiperspirant cosmetic products containing aromatic sulfonic acids
DE102013220771A1 (en) 2013-10-15 2015-04-16 Henkel Ag & Co. Kgaa Antiperspirant cosmetic products containing polycarboxylic acids
DE102013220767A1 (en) 2013-10-15 2015-04-16 Henkel Ag & Co. Kgaa Use of polysaccharides in antiperspirant cosmetic agents for textile care
DE102013220786A1 (en) 2013-10-15 2015-04-16 Henkel Ag & Co. Kgaa Antiperspirant cosmetic products containing amidosulfonic acids
DE102013220770A1 (en) 2013-10-15 2015-04-16 Henkel Ag & Co. Kgaa Antiperspirant cosmetic products containing polyphosphoric acids
DE102013225616A1 (en) 2013-12-11 2015-06-11 Henkel Ag & Co. Kgaa Antiperspirant cosmetic products containing lysozyme and / or bovine serum albumin and / or yoghurt protein
DE102013226812A1 (en) 2013-12-20 2015-06-25 Henkel Ag & Co. Kgaa Antiperspirant emulsions with improved adsorption
DE102014205199A1 (en) 2014-03-20 2014-10-23 Henkel Ag & Co. Kgaa Antiperspirant cosmetic compositions containing water-soluble polysaccharides
US9572758B2 (en) 2015-06-30 2017-02-21 Gulbrandsen Technologies, Inc. Method of making high performance activated aluminum sesquichlorohydrate powders
US20170128332A1 (en) * 2015-11-09 2017-05-11 Gulbrandsen Technologies, Inc. Activation and stabilization of basic aluminum chloride solution by zinc
DE102015225687A1 (en) 2015-12-17 2017-06-22 Henkel Ag & Co. Kgaa Propellant-free deodorant and / or antiperspirants with at least two different preservatives
DE102015225693A1 (en) 2015-12-17 2017-06-22 Henkel Ag & Co. Kgaa Propellant-free deodorant and / or antiperspirants with special preservative combinations
DE102015225958A1 (en) 2015-12-18 2017-06-22 Henkel Ag & Co. Kgaa Cosmetic compositions containing a combination of at least two different active ingredients
DE102015225876A1 (en) 2015-12-18 2017-06-22 Henkel Ag & Co. Kgaa "Deodorants containing specific cationic morpholino compounds in combination with certain active substances"
DE102015225971A1 (en) 2015-12-18 2017-06-22 Henkel Ag & Co. Kgaa A method for reducing perspiration-induced body odor using special protein hydrolysates
DE102015225892A1 (en) 2015-12-18 2016-10-27 Henkel Ag & Co. Kgaa Deodorants containing specific cyclic alcohols in combination with certain Deowirkstoffen
DE102016205332A1 (en) 2016-03-31 2017-10-05 Henkel Ag & Co. Kgaa Antiperspirant and / or deodorant cosmetic products with low emulsifier content
DE102016210037A1 (en) 2016-06-07 2017-12-07 Henkel Ag & Co. Kgaa "Highly effective antiperspirants with improved skin tolerance"
DE102017214798A1 (en) 2017-08-24 2019-02-28 Henkel Ag & Co. Kgaa Emulsifier system for microemulsions
DE102017214797A1 (en) 2017-08-24 2019-02-28 Henkel Ag & Co. Kgaa Emulsifier system for microemulsions with high skin tolerance
DE102017214799A1 (en) 2017-08-24 2019-02-28 Henkel Ag & Co. Kgaa Oil mixture for microemulsions
IT201900004805A1 (en) 2019-03-29 2020-09-29 Kalichem Srl ANTIPPIRANT AND DEODORANT COMPOSITIONS

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2814585A (en) 1954-04-30 1957-11-26 Procter & Gamble Buffered antiperspirant compositions
US2854382A (en) 1957-06-25 1958-09-30 Procter & Gamble Zirconyl hydroxy chloride antiperspirant compositions
CA972922A (en) 1970-07-30 1975-08-19 Raymond E. Bolich (Jr.) Aluminum-zirconium aerosol antiperspirant composition and process
US4435382A (en) * 1980-07-14 1984-03-06 Bristol-Myers Company Anhydrous alcoholic antiperspirant suspension composition containing certain aluminum or aluminum/zirconium salt glycine complexes
US4331609A (en) 1980-09-08 1982-05-25 The Procter & Gamble Company Antiperspirant composition
US4774079A (en) * 1980-12-15 1988-09-27 Bristol-Myers Company Antiperspirant composition containing aluminum chlorohydrate, aluminum chloride and an aluminum zirconium polychlorohydrate complex and method of use
CA1153313A (en) 1980-12-15 1983-09-06 Chung T. Shin Antiperspirant composition containing aluminum chlorohydrate, aluminum chloride and an aluminum zirconium polychlorohydrate complex and method of use
US4775528A (en) 1983-08-16 1988-10-04 The Gillette Company Antiperspirant composition
US4871525A (en) 1986-10-24 1989-10-03 Westwood Chemical Corporation Antiperspirant composition and method of preparation
GB8619553D0 (en) 1986-08-11 1986-09-24 Unilever Plc Antiperspirants
US5330751A (en) 1988-04-14 1994-07-19 The Gilette Company Antiperspirant and method of making same
US5348720A (en) * 1988-08-17 1994-09-20 The Mennen Company Basic aluminum antiperspirant active material having enhanced activity, antiperspirant active composition containing such material, and methods for preparation of such material and composition
DE69116580T2 (en) 1990-02-26 1996-06-20 Somerville Technology Group In Direct process for the production of activated antiperspirant salts
WO1992004281A1 (en) 1990-09-07 1992-03-19 Reheis, Incorporated Basic aluminum and aluminum/zirconium antiperspirants and method of making the same
US5225187A (en) 1991-02-15 1993-07-06 Somerville Technology Group, Inc. Process for preparing concentrated aluminum-zirconium solutions
US5320770A (en) * 1992-04-27 1994-06-14 Dow Corning Corporation Electrorheological (ER) fluid based on amino acid containing metal polyoxo-salts
ZA945542B (en) 1993-08-10 1995-05-26 Bristol Myers Squibb Co Novel zirconium salts and their synthesis
US5534246A (en) * 1994-08-29 1996-07-09 Helene Curtis, Inc. Topically-effective compositions
US5955064A (en) 1997-10-21 1999-09-21 Westwood Chemical Corporation Enhanced efficacy stable antiperspirant active solution and method of making same
US5997850C1 (en) 1997-10-29 2001-11-27 Colgate Palmolive Co Antiperspirant actives and formulations made therefrom
US6042816A (en) * 1998-08-19 2000-03-28 The Gillette Company Enhanced antiperspirant salts stabilized with calcium and concentrated aqueous solutions of such salts
US6126928A (en) 1999-08-24 2000-10-03 The Procter & Gamble Company Compositions containing solubilized, acid-enhanced antiperspirant active
US6451296B1 (en) 2000-02-01 2002-09-17 Zijun Li Enhanced efficacy aluminum-zirconium antiperspirants and methods for making
AR031108A1 (en) * 2000-06-19 2003-09-10 Colgate Palmolive Co A METHOD FOR IMPROVING THE ACTIVITY OF AN ALUMINUM OR ALUMINUM / CIRCONIUM SALT CONTAINING SMALL AND LARGE ALUMINUM SPECIES, SALES SO OBTAINED AND ANTI-TRANSPIRING AND / OR DEODORANT PRODUCTS PREPARED WITH SUCH IMPROVED SALTS
US6375937B1 (en) 2000-10-20 2002-04-23 Colgate-Palmolive Company Antiperspirant salts for enhanced cosmetic products
US6436381B1 (en) 2000-10-25 2002-08-20 The Gillette Company Aluminum-zirconium antiperspirant salts with high peak 5 al content

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